HuagongsheHuagongshe Chemistry Print Report · For research reference only
4'-bromo-[1,1'-Biphenyl]-4-carbonitrile → 4'-Furan-3-yl-biphenyl-4-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4'-bromo-[1,1'-Biphenyl]-4-carbonitrile | HCID 1394462 | — |
| Reactant | 3-(Biphenyl-4-yl)furan | HCID 18380293 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4'-Furan-3-yl-biphenyl-4-carbonitrile | HCID 18380417 | 53% |
Reaction Steps
As described in Example 1(a) for the preparation of 3-biphenyl-4-yl-furan, crude 4′-bromo-biphenyl-4-carbonitrile (200 mg, 0.775 mmol) and 3-fuiranboronic acid (see Thompson, W. J.; Gaudino, G. J. Org. Chem. 1984, 49, 5237-5243; 105 mg, 0.937 mmol) in MeOH (2 mL) were coupled to give a yellow solid, which was purified via preparative TLC. Elution with EtOAc:benzene (1:99) provided 100 mg (53%) of 4′-furan-3-yl-biphenyl-4-carbonitrile as a grey powder, mp 199-203° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06306892B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-d45b95a734d74dbea0a576924887c31a |
| Source note | uspto-grants-2001_10 |